TWI479042B - A method of plasma vapour deposition - Google Patents
A method of plasma vapour deposition Download PDFInfo
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- TWI479042B TWI479042B TW099101934A TW99101934A TWI479042B TW I479042 B TWI479042 B TW I479042B TW 099101934 A TW099101934 A TW 099101934A TW 99101934 A TW99101934 A TW 99101934A TW I479042 B TWI479042 B TW I479042B
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- Prior art keywords
- argon
- helium
- metal
- sputtering
- sccm
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- 238000000034 method Methods 0.000 title claims abstract description 40
- 230000008021 deposition Effects 0.000 title abstract description 8
- 229910052786 argon Inorganic materials 0.000 claims abstract description 41
- 229910052734 helium Inorganic materials 0.000 claims abstract description 26
- 238000004544 sputter deposition Methods 0.000 claims abstract description 20
- 229910052751 metal Inorganic materials 0.000 claims abstract description 18
- 239000002184 metal Substances 0.000 claims abstract description 18
- 238000000151 deposition Methods 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 80
- 239000001307 helium Substances 0.000 claims description 25
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 25
- 239000007789 gas Substances 0.000 claims description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 6
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 5
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052754 neon Inorganic materials 0.000 claims description 3
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052743 krypton Inorganic materials 0.000 claims 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 claims 1
- 238000002474 experimental method Methods 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 206010019909 Hernia Diseases 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/04—Coating on selected surface areas, e.g. using masks
- C23C14/046—Coating cavities or hollow spaces, e.g. interior of tubes; Infiltration of porous substrates
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/3471—Introduction of auxiliary energy into the plasma
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- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/35—Sputtering by application of a magnetic field, e.g. magnetron sputtering
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
- H01J37/3402—Gas-filled discharge tubes operating with cathodic sputtering using supplementary magnetic fields
- H01J37/3405—Magnetron sputtering
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/2855—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by physical means, e.g. sputtering, evaporation
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- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
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- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76853—Barrier, adhesion or liner layers characterized by particular after-treatment steps
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- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76871—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers
- H01L21/76873—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers for electroplating
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Abstract
Description
本發明係關於以完成使在一凹處基底之金屬再濺鍍至側壁上之方式將金屬電漿氣相沈積至一工作部件中之凹處的方法。 SUMMARY OF THE INVENTION The present invention is directed to a method of vapor depositing a metal plasma into a recess in a working component in a manner that accomplishes resputtering the metal of a recessed substrate onto the sidewall.
已知的是使用經離子化之金屬濺鍍技術包含一高功率失衡磁電管放電源。使用一藉由應用RF功率至該晶圓底座所引起之DC偏壓使該金屬離子被吸引至形成在一工作部件(如:一半導體晶圓)中一凹處之基底。如此賦予在該凹處中有經改善之底部及側壁覆蓋性。藉由再濺鍍已沈積在該基底之金屬至該凹處側壁之底部及中間部份上係被知道可達成進一步的改善。為了完成再濺鍍,需要在50至500伏特之範圍內的DC偏壓。該DC偏壓愈高,再濺鍍愈好且側壁覆蓋性則有改善。 It is known to use a ionized metal sputtering technique to include a high power unbalanced magnetron discharge source. The metal ions are attracted to a substrate formed in a recess in a working component (e.g., a semiconductor wafer) using a DC bias caused by application of RF power to the wafer carrier. This imparts improved bottom and sidewall coverage in the recess. Further improvements are known by re-sputtering the metal that has been deposited on the substrate to the bottom and intermediate portions of the sidewall of the recess. In order to complete re-sputtering, a DC bias in the range of 50 to 500 volts is required. The higher the DC bias voltage, the better the sputtering and the improved sidewall coverage.
即使是如此,現今之結果仍無法滿足所有的目的。 Even so, the results today are still not enough for all purposes.
由一觀點來看,本發明包含一以完成使在一凹處基底之金屬再濺鍍至側壁上之方式將金屬電漿氣相沈積至一工作部件中之凹處的方法,其係藉由以一濺鍍氣體濺鍍一金屬靶材,該濺鍍氣體之特徵在於該濺鍍氣體係氬氣和氦氣之混合物,當該氦氣和氬氣之比例係至少約10:1。 From one point of view, the present invention comprises a method of vapor-depositing a metal plasma into a recess in a working member in such a manner as to re-sputter the metal of a recessed substrate onto the sidewall. A metal target is sputtered with a sputtering gas characterized by a mixture of argon and helium in the sputtering gas system when the ratio of helium to argon is at least about 10:1.
較佳地該比例係約20:1。 Preferably the ratio is about 20:1.
氬氣的流率係<10sccm而氦氣的流率係>100sccm。因此舉例來說,該氦氣流率係約140sccm,而氬氣流率係約7sccm。 The flow rate of argon is <10 sccm and the flow rate of helium is >100 sccm. Thus, for example, the helium flow rate is about 140 sccm and the argon flow rate is about 7 sccm.
在以上之任一實例中,該金屬係銅。 In any of the above examples, the metal is copper.
在另一實施態樣中,該方法之特徵係在於氦及氬的混合係使得該靶材電流密度為至少約0.035A/cm2且較佳係約0.037A/cm2。 In another embodiment, the method is characterized by a mixing system of helium and argon such that the target current density is at least about 0.035 A/cm 2 and preferably about 0.037 A/cm 2 .
雖然該發明係已於上文被界定,其可被了解的是,其包括以上所提出或是以下所敘述之該等特徵的任何發明性合併。 Although the invention has been defined above, it will be appreciated that it includes any inventive combination of the features set forth above or described below.
該發明可以各種方式實行,且現在特定的實施態樣將參考所附之圖式以做為範例之方式而敘述,其中:第1圖係一DC磁電管離子化沉積濺鍍系統的剖面圖; 第2圖係一顯示如同用於入射在鉬及鎢靶材上之離子的轟擊能量和氣體類型之函數的二次電子發射的表格。此圖式係取自於Glow Discharge Processes,Chapmen,Wiley and Sons 1980;第3圖說明將氦氣添加至氬氣濺鍍過程中關於流率對靶材電流及電壓之變化;第4圖顯示對於一標準氬氣方法在一5:1溝渠結構中之側壁覆蓋;第5圖顯示對於一經最佳化之氦/氬方法之和第4圖的等同檢視;第6圖係一關於具有減少氦之氦/氬方法的等同檢視;第6(a)、(b)、(c)圖顯示氦/氬流分別對於沉積速率(校正因子)、壓力以及在晶圓內非均勻性之效果;以及第7圖係一具另一氦氣配方之和第5圖的等同檢視。 The invention may be embodied in a variety of ways, and the specific embodiments will now be described by way of example with reference to the accompanying drawings in which: FIG. 1 is a cross-sectional view of a DC magnetron ionization deposition sputtering system; Figure 2 is a table showing secondary electron emission as a function of the bombardment energy and gas type of ions incident on the molybdenum and tungsten targets. This pattern is taken from Glow Discharge Processes, Chapmen, Wiley and Sons 1980; Figure 3 illustrates the change in flow rate versus target current and voltage during the addition of helium to the argon sputtering process; Figure 4 shows A standard argon method covers the sidewalls of a 5:1 trench structure; Figure 5 shows an equivalent view of an optimized helium/argon method and Figure 4; and Figure 6 shows a reduction of flaws. An equivalent view of the helium/argon method; Figures 6(a), (b), and (c) show the effect of the helium/argon flow on the deposition rate (correction factor), pressure, and in-wafer non-uniformity, respectively; Figure 7 is an equivalent view of another hernia formula and Figure 5.
在一不平衡之DC磁電管離子化濺鍍沉積系統中,金屬及氣體離子化係經由金屬及氣體原子以在靶材表面所產生之二次電子碰撞而達成。該二次電子係藉由提供給該靶材表面之負偏壓而加速且達到高能量,典型地係200至1000eV。 In an unbalanced DC magnetron ionization sputter deposition system, metal and gas ionization is achieved by metal and gas atoms colliding with secondary electrons generated on the surface of the target. The secondary electrons are accelerated and reach high energy by a negative bias provided to the surface of the target, typically between 200 and 1000 eV.
這些高能量二次電子碰撞金屬及氣體原子或分子且產生離子。因此,若由該靶材所發射出之二次電子的數量可被增加,則會有離子化部份的增加,即為出自任何種類之離子對中性物之比例。 These high energy secondary electrons collide with metals and gas atoms or molecules and generate ions. Thus, if the amount of secondary electrons emitted by the target can be increased, there will be an increase in the ionized portion, i.e., the ratio of ions to neutral species of any kind.
如第2圖中所可見的,對於不同濺鍍氣體之二次電子特性係依據所使用之濺鍍氣體而變化。例如,相較於如氬及氪較重之氣體,氦及氖具有較高層次之二次電子放射。申請人遂了解到以氦或氖取代氬之濺鍍係有可能導致更多由該靶材所發出之二次電子及由此而來的離子化部份。 As can be seen in Figure 2, the secondary electronic properties for different sputtering gases vary depending on the sputtering gas used. For example, tantalum and niobium have a higher level of secondary electron emission than gases such as argon and helium. Applicants have learned that a sputtering system that replaces argon with helium or neon may result in more secondary electrons emitted by the target and the resulting ionized portion.
此效果已被該申請人藉由使用銅靶材以漸進地導入增加層次之氦流且減少氬流而研究,且其可看出當氦增加且氬減少時,由於在該靶材表面之二次電子形成使得電流增加。低層次的氬存在係被發現為必要以維持膜密度品質。 This effect has been investigated by the Applicant by using a copper target to progressively introduce increased levels of turbulence and reduce argon flow, and it can be seen that as the enthalpy increases and argon decreases, due to the surface of the target Sub-electron formation causes the current to increase. Low levels of argon present have been found to be necessary to maintain film density quality.
該申請人接著進行一使用第1圖之裝置以及以下第1表所顯示之方法條件的實驗。 The applicant then proceeded to an experiment using the apparatus of Figure 1 and the method conditions shown in Table 1 below.
此比較了在如第1圖之裝置上運作之標準僅用氬的方法及一其中氬流為7sccm而氦流為140sccm的氦/氬方法。該第一種方法所致之覆蓋係顯示在第4圖中,然而對於該第二種方法,該覆蓋係在第5圖中說明。該所致之階狀覆蓋係總結在以下第2表中。 This compares the standard argon-only method operating on the apparatus as in Figure 1 and a helium/argon process in which the argon flow is 7 sccm and the turbulent flow is 140 sccm. The overlay resulting from this first method is shown in Figure 4, however for this second method, the overlay is illustrated in Figure 5. The resulting step coverage is summarized in Table 2 below.
所見的是該氦/氬方法顯示出在側壁覆蓋係超越該僅用氬之方法的數值有5%絕對性、30%比例性的增加。 It is seen that the helium/argon method shows an 5% absolute, 30% proportional increase in the value of the sidewall covering system beyond the argon only method.
由第1表可見,對於該氦/氬方法,相較於該僅用氬之方法(標準),該平台DC偏壓只有增加30V(12%),儘管施加至該平台之RF功率已增加了165W(50%)。此顯示了該氦/氬方法具有較高層次的離子化,因為在該電漿中之正性離子將傾向於減少在該平台處所達成之負性DC偏壓。 As can be seen from Table 1, for the helium/argon method, the platform DC bias is only increased by 30V (12%) compared to the argon only method (standard), although the RF power applied to the platform has increased. 165W (50%). This shows that the helium/argon process has a higher level of ionization because the positive ions in the plasma will tend to reduce the negative DC bias achieved at the platform.
在第6圖中,係執行相同之方法,但這次是以75sccm之氦流而該結果係總結在以下第3表中。 In Figure 6, the same method was performed, but this time with a turbulent flow of 75 sccm and the results are summarized in Table 3 below.
由此可看出,比較140氦/7氬之方法及僅用氬之方法二者,減少氦流會造成側壁覆蓋的減少。這是因為在此實驗中,在該電漿中所產生之二次電子係因較低之氦流而減少。 It can be seen that comparing the 140 氦 / 7 argon method and the argon only method, reducing turbulence causes a reduction in sidewall coverage. This is because in this experiment, the secondary electrons generated in the plasma were reduced by lower turbulence.
實驗已顯示出,<10Sccm的氬係所需以維持該電漿且使得濺鍍該銅靶材得以發生。相反地,>100Sccm的氦流係所需以協助維持該電漿且提供額外的二次電子以增強在該結構底部處之濺鍍效果且因此改善側壁覆蓋。 Experiments have shown that <10 Sccm of argon is required to maintain the plasma and to cause sputtering of the copper target to occur. Conversely, a turbulence system of >100 Sccm is required to assist in maintaining the plasma and to provide additional secondary electrons to enhance the sputtering effect at the bottom of the structure and thus improve sidewall coverage.
在進一步的實驗中,該沉積速率、應力及晶圓內非均勻性係隨著改變之流而被監控,且該等結果係分別被顯示在第6(a) 至6(c)圖中。可見的是,雖然沉積速率隨著添加氦而下降,該7氬/140氦之方法係仍然足夠高於生產的目的。此種組合具有特別好的應力值以及可預期的均勻性。將被了解的是,減少的膜應力有助於避免銅膜從下方材料剝落。 In further experiments, the deposition rate, stress, and in-wafer non-uniformity were monitored as the flow of change, and the results were shown in Section 6(a), respectively. To 6 (c). It can be seen that although the deposition rate decreases with the addition of ruthenium, the 7 argon/140 方法 method is still sufficiently higher than the production purpose. This combination has particularly good stress values and predictable uniformity. It will be appreciated that reduced film stress helps to prevent the copper film from peeling off from the underlying material.
第7圖說明一減少之氦流隨著一增加之氬流,且該階狀覆蓋係再度減少,如以下第4表所呈現者。 Figure 7 illustrates a reduced turbulent flow with an increased argon flow and the step coverage is again reduced, as presented in Table 4 below.
因此,總結而論,可見的是,藉由使氦流率高於約100sccm且氬流率低於約10sccm即可達成相當大的改善。就以上所指出之理由,該7氬/140氦之方法造成一特別較佳的方法。 Thus, in summary, it can be seen that considerable improvement can be achieved by having a turbulent flow rate above about 100 sccm and an argon flow rate below about 10 sccm. For the reasons indicated above, the 7 argon/140 Torr method results in a particularly preferred method.
事實上,其可能更普遍適於陳述的是,就其所達成之成果而論,如同這些氣體之分壓應相對地維持在相應的常數,然而該實際流率可能在腔室和腔室之間有變化。下方第5表提出供用於該等實驗流率之等效分壓。 In fact, it may be more generally stated that, in terms of the results achieved, the partial pressures of these gases should be relatively constant at the corresponding constants, however the actual flow rate may be in the chamber and chamber. There are changes. Table 5 below presents the equivalent partial pressures for these experimental flow rates.
在該等實驗中所使用的金屬係銅。本發明方法對於鈦、鉭、金或釕應是相似的。 Metal-based copper used in these experiments. The process of the invention should be similar for titanium, tantalum, gold or rhenium.
第1圖係一DC磁電管離子化沉積濺鍍系統的剖面圖;第2圖係一顯示如同用於入射在鉬及鎢靶材上之離子的轟擊能量和氣體類型之函數的二次電子發射的表格。此圖式係取自於Glow Discharge Processes,Chapmen,Wiley and Sons 1980;第3圖說明將氦氣添加至氬氣濺鍍過程中關於流率對靶材電流及電壓之變化;第4圖顯示對於一標準氬氣方法在一5:1溝渠結構中之側壁覆蓋; 第5圖顯示對於一經最佳化之氦/氬方法之和第4圖的等同檢視;第6圖係一關於具有減少氦之氦/氬方法的等同檢視;第6(a)、(b)、(c)圖顯示氦/氬流分別對於沉積速率(校正因子)、應力以及在晶圓內非均勻性之效果;以及第7圖係一具另一氦氣配方之和第5圖的等同檢視。 Figure 1 is a cross-sectional view of a DC magnetron ionization deposition sputtering system; Figure 2 is a diagram showing secondary electron emission as a function of bombardment energy and gas type for ions incident on molybdenum and tungsten targets. Form. This pattern is taken from Glow Discharge Processes, Chapmen, Wiley and Sons 1980; Figure 3 illustrates the change in flow rate versus target current and voltage during the addition of helium to the argon sputtering process; Figure 4 shows A standard argon method is applied to the sidewall of a 5:1 trench structure; Figure 5 shows an equivalent view of an optimized helium/argon method and Figure 4; Figure 6 shows an equivalent view of a helium/argon method with reduced helium; 6(a), (b) (c) shows the effect of the helium/argon flow on the deposition rate (correction factor), stress, and in-wafer non-uniformity, respectively; and Figure 7 is the equivalent of another helium formulation and Figure 5. View.
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